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CN88100540A - Method for recovering propane and heavy hydrocarbons from hydrocarbon gas - Google Patents

Method for recovering propane and heavy hydrocarbons from hydrocarbon gas
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Publication number
CN88100540A
CN88100540ACN88100540.1ACN88100540ACN88100540ACN 88100540 ACN88100540 ACN 88100540ACN 88100540 ACN88100540 ACN 88100540ACN 88100540 ACN88100540 ACN 88100540A
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vapor
feed gas
stream
fractionation column
vapor fraction
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CN88100540.1A
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Chinese (zh)
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CN1007244B (en
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唐纳德·E·普里布
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Randall Corp
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Randall Corp
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Abstract

Translated fromChinese

一种从天然气或类似炼油厂气或含轻烃如甲烷和乙烷的反应气体物流中回收丙烷和重烃的深冷法。在公开的方法中,冷却待分离的气体可包括冷凝,在此情况下,冷凝物与蒸气分离,进入所有分馏塔的低部,出自分离器的已冷却蒸气被分成两股物流,其中一部分已分离的蒸气物流被膨胀,进入分馏塔中部,而另一部分已分离的蒸气物流经进一步冷却,以部分冷凝,被分离的冷凝液在来自第一膨胀作功机蒸气进料的上方进入分馏塔,而被分离的蒸气通过第二膨胀器膨胀,进入分馏塔的顶部,作为回流。A cryogenic process for the recovery of propane and heavy hydrocarbons from natural gas or similar refinery gas or reaction gas streams containing light hydrocarbons such as methane and ethane. In the disclosed method, cooling the gas to be separated may include condensation, in which case the condensate is separated from the vapor and enters the lower portion of any fractionation column, and the cooled vapor exiting the separator is split into two streams, a portion of which has been The separated vapor stream is expanded and enters the middle of the fractionation column while another part of the separated vapor stream is further cooled to partially condense, the separated condensate enters the fractionation column above the vapor feed from the first expansion work machine, The separated vapor is expanded through the second expander and enters the top of the fractionation column as reflux.

Description

Process for recovering propane and heavier hydrocarbons from hydrocarbon gas
This invention relates generally to processing hydrocarbon gas streams, such as natural gas or similar refinery gas or reaction gas streams, to recover therefrom a desired condensable portion, and more particularly to improving a gas cryogenic separation process to recover propane and heavy hydrocarbons from a hydrocarbon gas stream, such as natural gas or a similar refinery gas or reaction gas stream.
The recovery of these compounds from natural gas or similar refinery gases or reaction gas streams is always most economical due to market demand and price for propane and heavy hydrocarbon liquids. However, this is not the case and the demand and price fluctuations for ethane are so dramatic that it is economical to leave ethane in the combustible gas for a considerable period of time to recover only propane and heavier hydrocarbons, and also because of the location of some markets, the recovery of ethane is by no means an economic proposition. Accordingly, there is a need for a process for recovering propane and heavier hydrocarbons from a hydrocarbon gas stream while rejecting ethane and light components back to the residue or fuel gas.
U.S. patent nos. 4, 140, 504, 4, 157, 904 and 4, 278, 457 disclose several prior art cryogenic hydrocarbon separation processes. For example, in U.S. patent No. 4,157,904, a process for the cryogenic separation of a hydrocarbon gas stream to recover ethane and heavier hydrocarbons is disclosed, as described therein, with the gas to be separated being at about 900 pounds per inch gauge2Precooling at high pressure, partial condensation taking place and the condensate and vapour being separated. The first portion of the vapor is expanded to a low pressure and enters the demethanizer, and the second portion of the vapor is first cooled by heat exchange with the residue gas from the demethanizer and then enters the demethanizer either above or below the point of injection of the first portion of the expanded vapor by an expansion valve, depending on the exact temperature conditions. The cold humorous stream from the separator is further cooled and split into two streams, one stream being expanded to low pressure and forwarded to the lower section of the demethanizer, and the other stream being directed to the second stream from the previous separatorThe two portions of vapor are combined, re-cooled and expanded. Ethane recovery of 90% or more and propane recovery of 98% are described.
In most of the prior art processes described in the above patents, and particularly those designed primarily for high ethane recovery rather than ethane rejection from the processes described above, it can be seen that these prior art processes, without modification, are not suitable for the efficient recovery of propane and heavy hydrocarbons from mixed hydrocarbon gas streams while rejecting lighter hydrocarbon liquids, particularly ethane.
It is an object of the present invention to provide a cryogenic separation process for the recovery of propane and heavy hydrocarbons from a mixed hydrocarbon gas stream while rejecting light hydrocarbons, including ethane.
In the process of the invention, the feed gas is cooled to partial condensation by the residual gases, the condensate in the cooled feed gas is separated from the vapor and is expanded to a lower pressure by a valve and forwarded to the lower part of the column. The vapor is divided into two portions, the first portion of which is expanded to a low pressure by an expansion work machine and then fed to the column as an intermediate feed, the second portion of the vapor is further cooled by residual gas, so that part of the vapor is condensed, the vapor and liquid are separated from the cooled second portion of the vapor, the liquid is expanded through a valve to the intermediate portion of the low pressure feed column, and the remaining vapor is expanded to a low pressure by a second expansion work machine and forwarded to the top of the column as reflux. Partial condensation and separation of the vapor and liquid prior to the second expander produces a vapor containing a very small amount of propane, which is advantageously used as an overhead reflux feed. The power from the expansion work machine is used to compress the residue gas or feed gas to a high pressure.
The invention will be better understood from the following description of a preferred embodiment of the method according to the invention, with reference to the accompanying drawings, in which:
FIG. 1 is a schematic flow diagram of a process for carrying out the invention using two expansion work machines;
FIG. 2 shows the use of the present inventionOpen process, recovery efficiency and recompressor feet per million3Brake horsepower consumed per day (BHP/MMSCFD).
Referring to FIG. 1, the mixed hydrocarbon gas stream is at 485 lb/in2And 60 ° F into the flow. Feedgas stream 1 is pretreated as necessary to remove water and other compounds such as carbon dioxide or sulfur, andfeed gas stream 1 is compressed bycompressors 41 and 43 to provide a feed gas having 643 lbs/inch2A high pressurefeed gas stream 3 at a pressure and 105 DEG F,compressors 41 and 43 are connected to the shafts ofexpansion work machines 40 and 42, respectively, in such a way that the power provided by theexpansion work machines 40 and 42 is used to drive thecompressors 41 and 43.
Feed gas stream 3 is cooled to 25 ° F by passingresidue gas stream 18 inheat exchanger 25 at a pressure of 638 psig2The hydrocarbon components ofgas stream 3 are partially condensed and the condensate resulting from this cooling is separated from the remaining vapor inseparator 30 and enters the lower portion ofcolumn 90 through valve 80, with vapor stream 5 fromseparator 30 being separated intofirst vapor stream 7 andsecond vapor stream 8. Thevapor stream 7 is passed through anexpansion work machine 40 to a temperature of-55 ° F and a pressure of 249 lb/inch2A cooler partially condensed stream is then fed to the lower middle section ofcolumn 90 andvapor stream 8 is heat exchanged withcold residue gas 14 inheat exchanger 26, further cooled and partially condensed to form-104F and 631 lb/in2Is separated into avapor stream 12 and acondensate 13 byseparator 31. Thecondensate 13 is flashed to a pressure of 249 lb/in through valve 812And a temperature of-154F into the upper middle ofcolumn 90. Thevapor stream 12 is expanded to 249 lb/in by anexpansion work machine 422and-162F into the top of thecolumn 90.
Thefractionation column 90 connected to thereboiler 91 comprises a deethanizer column. The hydrocarbon liquid collected at the bottom of thefractionation column 90 exits thecolumn 90 through thereboiler 91 as aliquid hydrocarbon product 15. The heating raises the temperature of the bottoms liquid flowing throughreboiler 91 to remove any remaining lower by evaporationA lighter boiling light hydrocarbon, including ethane, but a non-vaporizing higher boiling propane and heavy hydrocarbon formingproduct stream 15 exits the bottom of thefractionation column 90 at a temperature of 147 c and a pressure of 252 psig2
Theresidue stream 14 from thefractionation column 90, which comprises residue gas, typically almost all of the methane produced by the separation, exits the top of thecolumn 90 at a temperature of-130F and a pressure of 249 lb/inch2. Theraffinate stream 14 is passed throughheat exchanger 26 to cool thevapor stream 8 leavingseparator 30, and throughheat exchanger 25 to cool thepressurized feed stream 3 supplied toseparator 30. During cooling ofvapor stream 8 andfeed gas stream 3,residue gas stream 14 is heated to a temperature of 100 ° F and a pressure of 239 lb/in2
The heatedresidue gas stream 19 exitingdownstream heat exchanger 25 is passed through arecompressor 50 to provide a pressurizedresidue gas stream 20 at a pressure of 490 psig2The temperature was 231 ℃ F. Therecompressor 50 is used to increase the pressure of the residual gas stream, which constitutes the processgas feed stream 1 free of the recovered heavy hydrocarbonliquid product stream 15, back to the pressure level of the incomingfeed gas stream 1.
To calculate the propane recovery capacity of the process of the invention, a computer simulation of the cryogenic separation process was performed, in which computer simulation the thermodynamic data used were the Soave-Redlich-kwong (SRK) K value, the stewed and the entropy. The efficiency of each of theexpansion machines 40 and 42 is assumed to be 80%, the efficiency of therecompressor 50 is assumed to be 75%, and the loss of the expansion machines is assumed to be 4% of the total power. In addition, a minimum temperature of approximately 5 ° F was used in all heat exchangers to calculate heat transfer effectiveness.
In addition, thefractionation column 90 used in the computer simulation has 20 theoretical plates and the power supplied from theexpansion work machines 40 and 42 is used to drive thefeed gas compressors 41 and 43, rather than therecompressor 50. The residue gas stream was brought to its desired outlet pressure of 490 psig2. In the computer simulation, vapor stream 5 fromseparator 30 was separated intovapor stream 7 and a vapor streamProduct 8 to obtain optimum propane recovery, it has been determined that separation of vapor stream 5 fromseparator 30 is optimum whenvapor stream 7 contains about 40% to 60% vapor stream 5 and, in addition, the ethane content ofliquid product stream 15 is controlled to be 2 mole%.
Thefeed gas stream 1 used in the computer simulation had the following composition:
helium 0.10
Nitrogen 1.26
Carbon dioxide 0.32
Methane 90.56
Ethane 4.37
Propane 2.23
Isobutane 0.30
N-butane 0.57
Isopentane 0.12
N-pentane 0.11
Hexane 0.04
Heptane 0.02
FIG. 2 provides the performance calculations made from such computer simulations, namely propane recovery expressed as percent propane infeed gas stream 1 and recompressor brake horsepower per million standard feet3Dependence of day (BHP/MMSCFD). Consumed recompressor brake horsepower per million standard feet3Gas flow/day is the power required to measure the pressure of theresidue gas stream 20 back to the pressure of thefeed gas stream 1. Thus, a plot of propane recovery versus recompressor brake horsepower provides a measure of the economic benefit potential of the process. As shown in FIG. 2, the method of the present invention consumes as little as one million standard feet per day of power from the recompressor3A high recovery of at least 98% propane was obtained for 42 brake horsepower. The propane recovery of the process of the invention illustrated in FIG. 1 for the above-claimed conditions is that of feed gas stream 1The alkane content was 98.4%.
As shown, the compressedfeed gas stream 3 is passed in heat exchange relationship with aresidue gas stream 14 from afractionation column 90. And may enter theseparator 30 after cooling. This cooling is necessary in carrying out the process of the invention to condense part of the heavy hydrocarbons in the feed gas, as a result of which the feed gas is particularly rich in propane and heavy hydrocarbons, and it is most desirable to achieve an optimum low temperature of the compressedfeed gas stream 3 using auxiliary refrigeration in addition to cooling by the residual gas, which can be accomplished by separating the pressurizedfeed gas stream 3 into two portions, one of which is cooled by heat exchange with theresidual gas stream 14 and the other of which is cooled by auxiliary refrigeration.
The process of the present invention may also be modified to recover a portion of the ethane in the feed gas by changing the operating conditions ofreboiler 91 so that the bottoms liquid passing throughreboiler 91 is heated to a temperature less than the boiling point of ethane at the existing liquid pressure. In this way, the relatively volatile light hydrocarbons, such as methane, are removed from the liquid inreboiler 91 by evaporation to produce a product stream rich in propane and heavy hydrocarbons and also containing a portion of the ethane in the feed gas.
Those skilled in the art will recognize that the specific pressures and temperatures of the feed gas streams toseparators 30 and 31, and the pressures and temperatures of the various steps in the process, will depend upon the conditions and properties of the gas to be processed, and the liquid hydrocarbons to be recovered from the feed stream in practicing the process of the present invention. It is therefore to be understood that the precise pressures and temperatures set forth in the specification are indicative of the best conditions presently contemplated in carrying out the process of the invention, and are not limiting of the process of the invention as set forth in the claims. Accordingly, this invention includes modifications thereto which would be obvious to those skilled in the art, and such modifications are intended to be within the spirit and scope of the appended claims.

Claims (5)

Translated fromChinese
1、一种通过分馏塔深冷分离混合烃进料气,从较轻烃残余物回收丙烷和重烃的方法,包括:1. A method for recovering propane and heavy hydrocarbons from a lighter hydrocarbon residue by cryogenically separating a mixed hydrocarbon feed gas in a fractionating tower, comprising:(a)压缩进料气使其增高压力;(a) compressing the feed gas to increase its pressure;(b)冷却加压的进料气体足以使其部分冷凝,由此从进料气体和进料气体的蒸气部分形成冷凝液,(b) cooling the pressurized feed gas sufficiently to partially condense it, thereby forming a condensate from the feed gas and the vapor portion of the feed gas,(c)将进料气体冷凝液和进料气体的蒸气部分分离,将进料气冷凝液送至分馏塔的较低部位;(c) separating the feed gas condensate from the vapor portion of the feed gas and sending the feed gas condensate to a lower portion of a fractionation column;(d)将已分离的进料气蒸气部分分成第一蒸气分流和第二蒸气分流,(d) dividing the separated feed gas vapor portion into a first vapor fraction stream and a second vapor fraction stream,(e)将所述第一蒸气分流在第一膨胀作功机中膨胀至低压,把已膨胀的第一蒸气分流供给分馏塔的中部;(e) expanding the first vapor fraction to a low pressure in a first expansion machine, and supplying the expanded first vapor fraction to a middle portion of a fractionation column;(f)进一步冷却所述第二蒸气分流至足以使其部分冷凝,以此从第二蒸气分流和第二蒸气分流的蒸气部分形成一种冷凝液;(f) further cooling the second vapor fraction stream sufficiently to partially condense it, thereby forming a condensate from the second vapor fraction stream and the vapor portion of the second vapor fraction stream;(g)将第二蒸气分流的冷凝液与其蒸气分离,将冷凝液送进分馏塔中部以上的部位,而已膨胀的第一蒸气分流被送至分馏塔中部;(g) separating the condensate of the second vapor fraction from its vapor and passing the condensate to a portion of a fractionation column above the middle portion, while the expanded first vapor fraction is passed to the middle portion of the fractionation column;(h)所述第二蒸气分流的蒸气部分在第二膨胀作功机中膨胀至低压,该已膨胀的第二蒸气分流的蒸气部分供给分馏塔的上部,在该处将第二蒸气分流冷凝液送进分馏塔内;(h) expanding the vapor portion of the second vapor fraction to a lower pressure in a second expander, and supplying the expanded vapor portion of the second vapor fraction to an upper portion of a fractionation column, where the second vapor fraction condensate is fed into the fractionation column;(i)加热聚集在分馏塔低部的烃液至足以蒸发其中所含的大部分轻烃以产生包括丙烷和重烃的产品烃液。(i) Heating the hydrocarbon liquid collected in the lower portion of the fractionation column sufficiently to vaporize a majority of the light hydrocarbons contained therein to produce a product hydrocarbon liquid comprising propane and heavy hydrocarbons.2、根据权利要求1所述方法,其中产品烃液的乙烷含量不大于2摩尔%左右。2. The process of claim 1, wherein the ethane content of the product hydrocarbon liquid is not greater than about 2 mole %.3、根据权利要求1所述方法,其中从分馏塔顶部流出的轻烃残余物流通过与第二蒸气分流热交换,冷却第二蒸气分流,以及与加压的进料气流热交换以冷却加压的进料气体物流,然后,该残余物流经再压缩以提高压力至步骤(a)压缩前的进料气体物流的近似压力。3. A process according to claim 1 wherein the light hydrocarbon residue stream exiting the top of the fractionation column is heat exchanged with the second vapor fraction stream to cool the second vapor fraction stream and with the pressurized feed gas stream to cool the pressurized feed gas stream, and then the residue stream is recompressed to increase its pressure to approximately the pressure of the feed gas stream prior to compression in step (a).4、根据权利要求1所述方法,其中第一和第二膨胀作功机各自驱动一个压缩机压缩进料气以提高其压力。4. The method according to claim 1, wherein the first and second expanders each drive a compressor to compress the feed gas to increase its pressure.5、根据权利要求1所述方法,其中第一蒸气分流包括已分离进料气总蒸气部分的40%至60%左右。5. The process of claim 1 wherein the first vapor fraction comprises from about 40% to about 60% of the total vapor portion of the separated feed gas.
CN88100540A1987-01-301988-01-30From the hydrocarbon gas, reclaim the method for propane and heavy hydrocarbonExpiredCN1007244B (en)

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US07/009,168US4752312A (en)1987-01-301987-01-30Hydrocarbon gas processing to recover propane and heavier hydrocarbons
US009,1681987-01-30

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CN88100540Atrue CN88100540A (en)1988-09-07
CN1007244B CN1007244B (en)1990-03-21

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CN (1)CN1007244B (en)
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CA (1)CA1297913C (en)

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CN101479549B (en)*2006-06-272011-08-10氟石科技公司 Ethane Recovery Methods and Configurations
CN102351625A (en)*2011-08-192012-02-15西安长庆科技工程有限责任公司Oil field associated gas ethane recovery system
CN101529188B (en)*2006-10-242012-06-13国际壳牌研究有限公司Method and apparatus for treating a hydrocarbon stream
CN101652617B (en)*2007-02-122013-07-03唐纳德·里欧·斯廷森Natural gas treatment system
CN104296499A (en)*2014-10-212015-01-21杭州中泰深冷技术股份有限公司Double-turbine boosting expansion machine propane dehydrogenation cold box separation system and technique
CN105157350A (en)*2015-10-232015-12-16重庆耐德工业股份有限公司Technology and system for removing heavy hydrocarbons in natural gas
CN111886464A (en)*2018-01-112020-11-031304338阿尔伯塔有限公司 Method for recovering LPG and condensate from refinery fuel gas streams
CN112781320A (en)*2019-11-052021-05-11东洋工程株式会社Method and apparatus for separating hydrocarbons

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CN101479549B (en)*2006-06-272011-08-10氟石科技公司 Ethane Recovery Methods and Configurations
CN101529188B (en)*2006-10-242012-06-13国际壳牌研究有限公司Method and apparatus for treating a hydrocarbon stream
CN101652617B (en)*2007-02-122013-07-03唐纳德·里欧·斯廷森Natural gas treatment system
CN102351625A (en)*2011-08-192012-02-15西安长庆科技工程有限责任公司Oil field associated gas ethane recovery system
CN102351625B (en)*2011-08-192013-11-27西安长庆科技工程有限责任公司Oil field associated gas ethane recovery system
CN104296499A (en)*2014-10-212015-01-21杭州中泰深冷技术股份有限公司Double-turbine boosting expansion machine propane dehydrogenation cold box separation system and technique
CN104296499B (en)*2014-10-212016-03-23杭州中泰深冷技术股份有限公司A kind of two turbine booster expansion machine dehydrogenating propane ice chest piece-rate system and technique thereof
CN105157350A (en)*2015-10-232015-12-16重庆耐德工业股份有限公司Technology and system for removing heavy hydrocarbons in natural gas
CN111886464A (en)*2018-01-112020-11-031304338阿尔伯塔有限公司 Method for recovering LPG and condensate from refinery fuel gas streams
CN112781320A (en)*2019-11-052021-05-11东洋工程株式会社Method and apparatus for separating hydrocarbons

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CN1007244B (en)1990-03-21
AU591447B2 (en)1989-11-30
AU1110188A (en)1988-08-04
CA1297913C (en)1992-03-24
US4752312A (en)1988-06-21

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